Tag Content
SG ID
SG00009350 
UniProt Accession
Theoretical PI
6.87  
Molecular Weight
36587 Da  
Genbank Nucleotide ID
Genbank Protein ID
Gene Name
Akr1a1 
Gene Synonyms/Alias
Akr1a4 
Protein Name
Alcohol dehydrogenase [NADP(+)] 
Protein Synonyms/Alias
EC=1.1.1.2 Aldehyde reductase; Aldo-keto reductase family 1 member A1; 
Organism
Mus musculus (Mouse) 
NCBI Taxonomy ID
10090 
Chromosome Location
chr:4;116309115-116324285;-1
View in Ensembl genome browser  
Function in Stage
Uncertain 
Function in Cell Type
Uncertain 
Probability (GAS) of Function in Spermatogenesis
0.141579134 
The probability was calculated by GAS algorithm, ranging from 0 to 1. The closer it is to 1, the more possibly it functions in spermatogenesis.
Description
Temporarily unavailable 
Abstract of related literatures
1. The aldo-keto reductase superfamily catalyzes the reduction of a broad range of aldehydes and ketones to their corresponding alcohols. Here we report the cloning of the mouse aldehyde reductase cDNA and its embryonic pattern of expression. From stages E7.5 to E13.5 the gene encoding for this enzyme is expressed at high levels in several tissues, including the neural ectoderm, gut endoderm, somites, branchial arches, otic vesicles, limb buds, and tail bud. In adult mice aldehyde reductase was expressed in all tissues examined. PMID: [10842086] 

2. This study describes comprehensive polling of transcription start and termination sites and analysis of previously unidentified full-length complementary DNAs derived from the mouse genome. We identify the 5' and 3' boundaries of 181,047 transcripts with extensive variation in transcripts arising from alternative promoter usage, splicing, and polyadenylation. There are 16,247 new mouse protein-coding transcripts, including 5154 encoding previously unidentified proteins. Genomic mapping of the transcriptome reveals transcriptional forests, with overlapping transcription on both strands, separated by deserts in which few transcripts are observed. The data provide a comprehensive platform for the comparative analysis of mammalian transcriptional regulation in differentiation and development. PMID: [16141072] 

3. The National Institutes of Health's Mammalian Gene Collection (MGC) project was designed to generate and sequence a publicly accessible cDNA resource containing a complete open reading frame (ORF) for every human and mouse gene. The project initially used a random strategy to select clones from a large number of cDNA libraries from diverse tissues. Candidate clones were chosen based on 5'-EST sequences, and then fully sequenced to high accuracy and analyzed by algorithms developed for this project. Currently, more than 11,000 human and 10,000 mouse genes are represented in MGC by at least one clone with a full ORF. The random selection approach is now reaching a saturation point, and a transition to protocols targeted at the missing transcripts is now required to complete the mouse and human collections. Comparison of the sequence of the MGC clones to reference genome sequences reveals that most cDNA clones are of very high sequence quality, although it is likely that some cDNAs may carry missense variants as a consequence of experimental artifact, such as PCR, cloning, or reverse transcriptase errors. Recently, a rat cDNA component was added to the project, and ongoing frog (Xenopus) and zebrafish (Danio) cDNA projects were expanded to take advantage of the high-throughput MGC pipeline. PMID: [15489334] 

4. In this study we describe changes of gene expression that occur in the basolateral complex of the mouse amygdala (BLA) during the formation of fear memory. Through the combination of a behavioral training scheme with polymerase chain reaction-based expression analysis (subtractive hybridization and virtual Northern analysis) we were able to identify various gene products that are increased in expression after Pavlovian fear conditioning and are of potential significance for neural plasticity and information storage in the amygdala. In particular, a key enzyme of monoamine metabolism, aldehyde reductase, and the protein sorting and ubiquitination factor Praja1, showed pronounced and learning-specific induction six hours after fear conditioning training. Aldehyde reductase and Praja1, including a novel alternatively spliced isoform termed Praja1a, were induced in the BLA depending on the emotional stimulus presented and showed different expression levels in response to associative conditioning, training stress, and experience of conditioned fear. Stress and fear were further found to induce various signal transduction factors (transthyretin, phosphodiesterase1, protein kinase inhibitor-alpha) and structural reorganization factors (e.g., E2-ubiquitin conjugating enzyme, neuroligin1, actin, UDP-galactose transporter) during training. Our results show that the formation of Pavlovian fear memory is associated with changes of gene expression in the BLA, which may contribute to neural plasticity and the processing of information about both conditioned and unconditioned fear stimuli. PMID: [11533224] 

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Function
Catalyzes the NADPH-dependent reduction of a variety ofaromatic and aliphatic aldehydes to their corresponding alcohols.Catalyzes the reduction of mevaldate to mevalonic acid and ofglyceraldehyde to glycerol. Has broad substrate specificity. Playsa role in the activation of procarcinogens, such as polycyclicaromatic hydrocarbon trans-dihydrodiols, and in the metabolism ofvarious xenobiotics and drugs (By similarity). 
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Subcellular Location
 
Tissue Specificity
Widely expressed. 
Gene Ontology
GO IDGO termEvidence
GO:0016324 C:apical plasma membrane IDA:MGI.
GO:0005829 C:cytosol IDA:MGI.
GO:0004032 F:alditol:NADP+ 1-oxidoreductase activity IDA:MGI.
GO:0047939 F:L-glucuronate reductase activity IDA:MGI.
GO:0046185 P:aldehyde catabolic process IDA:MGI.
GO:0042840 P:D-glucuronate catabolic process IDA:MGI.
GO:0019853 P:L-ascorbic acid biosynthetic process IDA:MGI.
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Interpro
IPR001395;    Aldo/ket_red.
IPR018170;    Aldo/ket_reductase_CS.
IPR020471;    Aldo/keto_reductase_subgr.
IPR023210;    NADP_OxRdtase_dom.
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Pfam
PF00248;    Aldo_ket_red;    1.
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SMART
PROSITE
PS00798;    ALDOKETO_REDUCTASE_1;    1.
PS00062;    ALDOKETO_REDUCTASE_2;    1.
PS00063;    ALDOKETO_REDUCTASE_3;    1.
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PRINTS
PR00069;    ALDKETRDTASE.;   
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Created Date
18-Oct-2012 
Record Type
GAS predicted 
Sequence Annotation
INIT_MET      1      1       Removed.
CHAIN         2    325       Alcohol dehydrogenase [NADP(+)].
                             /FTId=PRO_0000124618.
NP_BIND      11     20       NADP (Potential).
NP_BIND     211    273       NADP (By similarity).
ACT_SITE     50     50       Proton donor (By similarity).
BINDING     113    113       Substrate (By similarity).
SITE         80     80       Lowers pKa of active site Tyr (By
                             similarity).
MOD_RES       2      2       N-acetylthreonine.
CONFLICT     54     54       T -> A (in Ref. 2; BAB27586).
CONFLICT     60     60       L -> P (in Ref. 2; BAB27915).
CONFLICT     95     95       L -> I (in Ref. 2; BAB27883/BAB27767).
CONFLICT    120    120       R -> L (in Ref. 2; BAB27909).
CONFLICT    284    284       E -> G (in Ref. 2; BAB27437).
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Nucleotide Sequence
Length: 1320 bp   Go to nucleotide: FASTA
Protein Sequence
Length: 325 bp   Go to amino acid: FASTA
The verified Protein-Protein interaction information
UniProt
Gene Symbol Ref Databases
CdiptString 
CdiptString 
Other Protein-Protein interaction resources
String database  
View Microarray data
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